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US4150169A - Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating - Google Patents

Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating Download PDF

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Publication number
US4150169A
US4150169A US05/864,464 US86446477A US4150169A US 4150169 A US4150169 A US 4150169A US 86446477 A US86446477 A US 86446477A US 4150169 A US4150169 A US 4150169A
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United States
Prior art keywords
substrate
coating
embossed
liquid
tile
Prior art date
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Expired - Lifetime
Application number
US05/864,464
Inventor
George E. Bagley
Robert H. Byers
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Armstrong World Industries Inc
Original Assignee
Armstrong Cork Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Armstrong Cork Co filed Critical Armstrong Cork Co
Priority to US05/864,464 priority Critical patent/US4150169A/en
Priority to DE2840581A priority patent/DE2840581C3/en
Priority to AU40088/78A priority patent/AU504396B1/en
Priority to SE7809967A priority patent/SE431831C/en
Priority to DK424478A priority patent/DK424478A/en
Priority to LU80284A priority patent/LU80284A1/en
Priority to CA312,443A priority patent/CA1101795A/en
Priority to BE78190881A priority patent/BE870980A/en
Priority to FR7830157A priority patent/FR2413135A1/en
Priority to NO783906A priority patent/NO152362C/en
Priority to JP15430678A priority patent/JPS5494565A/en
Priority to GB7849720A priority patent/GB2010700B/en
Priority to NL7812536.A priority patent/NL166994C/en
Application granted granted Critical
Publication of US4150169A publication Critical patent/US4150169A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/10Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by other chemical means
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N3/06Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products
    • D06N3/08Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products with a finishing layer consisting of polyacrylates, polyamides or polyurethanes or polyester

Definitions

  • This invention relates to a manufacturing method for providing an embossed thermoplastic surface covering with a photopolymerized wear layer.
  • the coating applied by the curtain coater is compatible and curable with acrylate monomers.
  • FIG. 1 illustrates an embossed coated tile manufactured in accordance with the practice of the prior art, showing the occluded air bubbles immediately behind the leading edge of the deep valleys in the machine direction and in the cured coating;
  • FIG. 2 illustrates a coated embossed tile produced in accordance with this invention
  • FIG. 3 diagrammatically illustrates the line set-up for manufacturing coated embossed vinyl substrates in accordance with this invention.
  • FIG. 1 illustrates in cross section an embossed vinyl-asbestos tile substrate 5 having a photopolymerizable coating 6 and occluded air bubbles as shown by the numeral 7.
  • FIG. 2 illustrates a tile prepared in accordance with the invention, including the embossed vinyl-asbestos tile substrate 5 and the photopolymerized coating 6.
  • FIG. 3 The method for producing the coated tile in accordance with the invention is diagrammatically illustrated in FIG. 3.
  • an embossed vinyl-asbestos tile substrate 13 is first passed beneath a Schmutch printer 8, which applies a liquid acrylate coating from a reservoir 9 onto the surface of the tile, the coating being squeezed down into the valleys 13, to thoroughly wet the embossed tile substrate.
  • the Schmutch printer has a wooden roll 10 which picks up the liquid from the reservoir 9 and transfers it to an etched chrome-plated roll 11 (Anilox Roll) which, in turn, transfers the coating onto a rubber roll 12 which is in contact with the tile passing thereunder.
  • a steel back-up roll 16 forms a nip opening with conveyor 14 and roll 12.
  • Conveyor 17 conveys the tile underneath the curtain coater 18, the curtain coater applying a curtain of liquid onto the tile, illustrated by numeral 22, with the excess liquid going into a reservoir 20, the tile, after being coated, is picked up by conveyor 21 which, in turn, transfers the tile to conveyor 24 which conveys the tile under a conventional photocuring system, in this instance, a battery of four, 200-watt per inch, medium pressure mercury arc lamps.
  • the following is an example of a 100% reactive photopolymerizable coating which cures to yield a tough, clear, mar-resistant coating when subjected to a source of ultraviolet radiation.
  • the trimethylolpropane diallyl ether is reacted with two equivalents of 4,4' diisocyanato-dicyclohexyl methane using 0.59 grams of dibutyltin dilaurate catalyst at a temperature of about 80° C. for one hour.
  • the allyl diglycol carbonate and the polycaprolactone triol are then added and reacted at 80° C. until there are no free --NCO groups.
  • the trimethylolpropane tris(beta-mercaptoproprionate), phosphorous acid, diethoxyacetophenone and pyrogallol are then mixed with the coating.
  • the coating as prepared, has a viscosity of about 6000 centipoises at 25° C. It is heated to about 170° F. in the curtain coater, giving a coating viscosity of about 900 centipoises.
  • the prewetting liquid has a viscosity of about 21 centipoises and is applied at room temperature.
  • the prewetting liquid is fed to the reservoir 9, where it is picked up by the wooden roll 10.
  • the overall etched roll 11 picks up a measured amount of liquid from roll 10, the amount determined by the extent of etching, in this instance, approximately 3000 cells per square inch are etched into the chrome-plated printing roll.
  • the measured amount is transferred to the rubber roll 12 and, at a speed of about 110 feet per minute, results in an application of one gram per square foot of embossed tile fed under the printer 8.
  • a one foot by one foot standard commercial embossed vinyl-asbestos tile 13 is fed through the printer 8 at a speed of 110 feet per minute on conveyor 14 in the machine direction indicated by the arrow 15.
  • the rubber roll 14 transfers sufficient liquid of the formulation of Example 2 at the nip established by roll 12 and back-up roll 16 to give a wet pick-up of a total of about one gram of liquid, most of which is forced into the valleys to thoroughly wet out all the depressions indicated by the numerals 13'.
  • the wetted tile 13 is then transported by conveyors 17 and 21 beneath the curtain coater 18 at a line speed of about 400 feet per minute, where a curtain 19 of the photopolymerizable coating of Example 1 is applied wet-on-wet to provide an overall coating pick-up 22' on tile 22 of about 11 grams or an even overall coating thickness of about 4 mils (0.004 inches or 1000 microns).
  • the coated tile 22 is then picked up by the conveyor 24 and transported under an ultraviolet light source 23 comprised of a battery of four in-line, 200 watt per inch, medium pressure mercury arc lamps at a line speed of 13.2 feet per minute. This dosage of ultraviolet light cures both coatings and yields an embossed tile with an overall clear 4 mil thick film which is tough and mar-resistant. No air bubbles are visible in the coating.
  • FIG. 1 shows a cross-sectional view of an embossed vinyl-asbestos tile substrate 5 having a photopolymerized coating 6 with occluded air bubbles 7.
  • FIG. 2 shows the same tile wherein a prewetting liquid has first been applied at the printer 8 before coating at the curtain coater 18 and curing at 23.
  • a further example of a wetting liquid that may be used in the practice of this invention is as follows:
  • the above liquid as formulated, has a viscosity of about 13 centipoises at 30° C. It works equally as well as the coating of Example 2 in prewetting the embossed substrate to eliminate air bubbles in the cured coated tile and is fully compatible and curable with the ultraviolet curable coating of Example 1.
  • Acrylate diluents comprise a major component of most ultraviolet light curable coatings, and the formulations of Examples 2 and 3 are fully compatible with such coatings.
  • the prewetting liquid should be formulated to give a viscosity in the range of about 10 to 100 centipoises and should consist essentially of a liquid mono, di- or tri-ethylenically unsaturated acrylate component together with sufficient photopolymerization initiator to allow polymerization at the ultraviolet light curing stage.
  • a viscosity in the range of about 10 to 100 centipoises and should consist essentially of a liquid mono, di- or tri-ethylenically unsaturated acrylate component together with sufficient photopolymerization initiator to allow polymerization at the ultraviolet light curing stage.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Laminated Bodies (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Shaping Of Tube Ends By Bending Or Straightening (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Vehicle Step Arrangements And Article Storage (AREA)
  • Paints Or Removers (AREA)
  • Finishing Walls (AREA)
  • Coating Apparatus (AREA)

Abstract

In a method for manufacturing an embossed thermoplastic surface covering wherein a 100% reactive photopolymerizable coating is applied to the embossed thermoplastic substrate, the improvement comprising prewetting the valleys of the embossed substrate with a liquid consisting essentially of an acrylate monomer or a mixture of acrylate monomers and sufficient photoinitiator to initiate polymerization when the coated substrate is subjected to ultraviolet radiation.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a manufacturing method for providing an embossed thermoplastic surface covering with a photopolymerized wear layer.
2. Description of the Prior Art
The desirability of protecting vinyl substrates such as thermoplastic vinyl-asbestos tile and decorative thermoplastic sheet goods utilized as floor coverings has been well recognized, and recently such substrates, protected by clear, tough, mar-resistant coatings, which are substantially 100% reactive and photocured have become widely available. For example, U.S. Pat. No. 3,485,732 has suggested radiation curable coating compositions for application to plastic substrates such as linoleum, and U.S. Pat. No. 3,924,023 suggests the application of photopolymerizable coatings to vinyl-asbestos substrates. It is substrates of the latter type, which have first been embossed, with which this invention is illustrated, although it will be readily evident that the invention has application in coating any embossed thermoplastic substrate.
It has been discovered that when an embossed vinyl substrate, particularly adapted for surface coverings such as floors, is coated with conventional, photopolymerizable coating compositions utilizing a curtain coater to apply the photopolymerizable coating to the substrate, the application of conventional coatings of about 2 to 5 mils results in the occlusion of air bubbles within the coating along the leading edge of the deeper valleys of the vinyl substrate, i.e., those edges which first pass beneath the curtain coater. Such bubbles can prove to be highly disadvantageous if they, in turn, are near or at the upper surface of the coating in that, should they puncture or break under wear conditions, they provide sites for dirt entrapment. Since the preferred coatings are essentially 100% reactive, they are generally highly viscous, and when subjected to an ultraviolet light cure, any occluded air will become permanently entrapped in the coating at the time of cure.
SUMMARY OF THE INVENTION
It is an object of our invention to eliminate the air bubbles in the coating. This is accomplished by prewetting the valleys of the embossed substrate with a liquid having a viscosity between about 10 centipoises and 100 centipoises before curtain coating the substrate, said liquid consisting essentially of an acrylate monomer or mixture of acrylate monomers and sufficient photoinitiator to initiate polymerization when the curtain coated substrate is subjected to ultraviolet radiation. The coating applied by the curtain coater is compatible and curable with acrylate monomers.
DESCRIPTION OF THE DRAWINGS
In the drawings, FIG. 1 illustrates an embossed coated tile manufactured in accordance with the practice of the prior art, showing the occluded air bubbles immediately behind the leading edge of the deep valleys in the machine direction and in the cured coating;
FIG. 2 illustrates a coated embossed tile produced in accordance with this invention; and
FIG. 3 diagrammatically illustrates the line set-up for manufacturing coated embossed vinyl substrates in accordance with this invention.
DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
By way of example, this invention will be described in connection with the manufacture of an embossed vinyl asbestos tile substrate, although it will be obvious that the invention is applicable to embossed thermoplastic substrates, generally, either in tile or sheet form.
With reference to the drawings, FIG. 1 illustrates in cross section an embossed vinyl-asbestos tile substrate 5 having a photopolymerizable coating 6 and occluded air bubbles as shown by the numeral 7. FIG. 2 illustrates a tile prepared in accordance with the invention, including the embossed vinyl-asbestos tile substrate 5 and the photopolymerized coating 6.
The method for producing the coated tile in accordance with the invention is diagrammatically illustrated in FIG. 3. As shown in FIG. 3, an embossed vinyl-asbestos tile substrate 13 is first passed beneath a Schmutch printer 8, which applies a liquid acrylate coating from a reservoir 9 onto the surface of the tile, the coating being squeezed down into the valleys 13, to thoroughly wet the embossed tile substrate. The Schmutch printer has a wooden roll 10 which picks up the liquid from the reservoir 9 and transfers it to an etched chrome-plated roll 11 (Anilox Roll) which, in turn, transfers the coating onto a rubber roll 12 which is in contact with the tile passing thereunder. A steel back-up roll 16 forms a nip opening with conveyor 14 and roll 12. The machine direction is illustrated by the arrow 15 and conveyor 14 carries the tile underneath the printer 8 and onto conveyor 17. Conveyor 17 conveys the tile underneath the curtain coater 18, the curtain coater applying a curtain of liquid onto the tile, illustrated by numeral 22, with the excess liquid going into a reservoir 20, the tile, after being coated, is picked up by conveyor 21 which, in turn, transfers the tile to conveyor 24 which conveys the tile under a conventional photocuring system, in this instance, a battery of four, 200-watt per inch, medium pressure mercury arc lamps.
The following is an example of a 100% reactive photopolymerizable coating which cures to yield a tough, clear, mar-resistant coating when subjected to a source of ultraviolet radiation.
EXAMPLE 1
______________________________________                                    
Ingredient            Parts by weight (gms)                               
______________________________________                                    
4,4' diisocyanato dicyclohexyl                                            
                      251.1                                               
methane                                                                   
Trimethylolpropane diallyl ether                                          
                      254.2                                               
Allyl diglycol carbonate                                                  
                      76.0                                                
Polycaprolactone triol* (Union Carbide                                    
                      68.2                                                
PCP0301 - molecular weight 300,                                           
hydroxy number 560)                                                       
Catalyst (Dibutyltin dilaurate)                                           
                      0.59                                                
Trimethylolpropane Tris(beta-mercapto-                                    
propionate)           339.7                                               
Phosphorous Acid      0.2                                                 
Diethoxyacetophenone  9.8                                                 
Pyrogallol            .1                                                  
______________________________________                                    
 *The polycaprolactone diol is prepared by polymerizing                   
 epsilon-caprolactone with trimethylol propane. (U.S. Patent 2,914,556)   
In preparing the coating, the trimethylolpropane diallyl ether is reacted with two equivalents of 4,4' diisocyanato-dicyclohexyl methane using 0.59 grams of dibutyltin dilaurate catalyst at a temperature of about 80° C. for one hour. The allyl diglycol carbonate and the polycaprolactone triol are then added and reacted at 80° C. until there are no free --NCO groups. The trimethylolpropane tris(beta-mercaptoproprionate), phosphorous acid, diethoxyacetophenone and pyrogallol are then mixed with the coating.
The coating, as prepared, has a viscosity of about 6000 centipoises at 25° C. It is heated to about 170° F. in the curtain coater, giving a coating viscosity of about 900 centipoises.
The following is an example of a prewetting liquid which may be used in the practice of this invention:
EXAMPLE 2
______________________________________                                    
Ingredients           Parts by weight (gms)                               
______________________________________                                    
Trimethylolpropane triacrylate                                            
                      75                                                  
2-ethylhexyl acrylate 25                                                  
Methyl diethanolamine 3                                                   
Benzophenone          3                                                   
______________________________________                                    
At 30° C., the prewetting liquid has a viscosity of about 21 centipoises and is applied at room temperature.
With reference to the drawing, wherein the production line is diagrammatically illustrated, the prewetting liquid is fed to the reservoir 9, where it is picked up by the wooden roll 10. The overall etched roll 11 picks up a measured amount of liquid from roll 10, the amount determined by the extent of etching, in this instance, approximately 3000 cells per square inch are etched into the chrome-plated printing roll. The measured amount is transferred to the rubber roll 12 and, at a speed of about 110 feet per minute, results in an application of one gram per square foot of embossed tile fed under the printer 8.
A one foot by one foot standard commercial embossed vinyl-asbestos tile 13 is fed through the printer 8 at a speed of 110 feet per minute on conveyor 14 in the machine direction indicated by the arrow 15. The rubber roll 14 transfers sufficient liquid of the formulation of Example 2 at the nip established by roll 12 and back-up roll 16 to give a wet pick-up of a total of about one gram of liquid, most of which is forced into the valleys to thoroughly wet out all the depressions indicated by the numerals 13'. The wetted tile 13 is then transported by conveyors 17 and 21 beneath the curtain coater 18 at a line speed of about 400 feet per minute, where a curtain 19 of the photopolymerizable coating of Example 1 is applied wet-on-wet to provide an overall coating pick-up 22' on tile 22 of about 11 grams or an even overall coating thickness of about 4 mils (0.004 inches or 1000 microns). The coated tile 22 is then picked up by the conveyor 24 and transported under an ultraviolet light source 23 comprised of a battery of four in-line, 200 watt per inch, medium pressure mercury arc lamps at a line speed of 13.2 feet per minute. This dosage of ultraviolet light cures both coatings and yields an embossed tile with an overall clear 4 mil thick film which is tough and mar-resistant. No air bubbles are visible in the coating.
When the tile is fed directly to the curtain coater 18 by passing the printer 8, bubbles of air are occluded by the viscous coating immediately behind the leading edge of the valleys 13'. This is illustrated in FIG. 1, which shows a cross-sectional view of an embossed vinyl-asbestos tile substrate 5 having a photopolymerized coating 6 with occluded air bubbles 7. FIG. 2 shows the same tile wherein a prewetting liquid has first been applied at the printer 8 before coating at the curtain coater 18 and curing at 23.
A further example of a wetting liquid that may be used in the practice of this invention is as follows:
EXAMPLE 3
______________________________________                                    
Ingredient            Parts by weight (gms)                               
______________________________________                                    
1,6-hexanediol diacrylate                                                 
                      99.0                                                
Benzoin isobutyl ether                                                    
                      1.0                                                 
______________________________________                                    
The above liquid, as formulated, has a viscosity of about 13 centipoises at 30° C. It works equally as well as the coating of Example 2 in prewetting the embossed substrate to eliminate air bubbles in the cured coated tile and is fully compatible and curable with the ultraviolet curable coating of Example 1.
Acrylate diluents comprise a major component of most ultraviolet light curable coatings, and the formulations of Examples 2 and 3 are fully compatible with such coatings.
Generally, the prewetting liquid should be formulated to give a viscosity in the range of about 10 to 100 centipoises and should consist essentially of a liquid mono, di- or tri-ethylenically unsaturated acrylate component together with sufficient photopolymerization initiator to allow polymerization at the ultraviolet light curing stage. Preferably between about 1/2 gram to 2 grams per square foot of embossed substrate are utilized to ensure that the valleys are fully prewetted and that the properties of the wear layer are not adversely affected.

Claims (2)

What is claimed is:
1. In a method for manufacturing an embossed thermoplastic surface covering having a clear, durable, tough, mar-resistant photopolymerized wear layer wherein an embossed substrate is coated by passing the substrate beneath a curtain coater which applies a 100% reactive photopolymerizable coating to the substrate, said coating being compatible and curable with acrylate monomers, and wherein the coated substrate is cured by subjecting the coated substrate to a source of ultraviolet radiation, the improvement comprising:
prewetting the valleys of the embossed substrate with a liquid having a viscosity of between about 10 centipoises and 100 centipoises before curtain coating the substrate, said liquid consisting essentially of an acrylate monomer or a mixture of acrylate monomers and sufficient photoinitiator to initiate polymerization when the curtain coated substrate is subjected to ultraviolet radiation.
2. The method in accordance with claim 1 in which between about 1/2 to 2 grams per square foot of said liquid is used to prewet the substrate.
US05/864,464 1977-12-27 1977-12-27 Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating Expired - Lifetime US4150169A (en)

Priority Applications (13)

Application Number Priority Date Filing Date Title
US05/864,464 US4150169A (en) 1977-12-27 1977-12-27 Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating
DE2840581A DE2840581C3 (en) 1977-12-27 1978-09-18 Method for producing a structured floor covering
AU40088/78A AU504396B1 (en) 1977-12-27 1978-09-22 Improved manufacture of embossed vinyl coating
SE7809967A SE431831C (en) 1977-12-27 1978-09-22 VIEW TO MAKE A THERMOPLAST EXISTING PREGNANT FLOOR COVERING WITH A CLEAR, AGE-RESISTANT, HEART, TONE-RESISTANT PHOTOPOLYMERIZED COATING LAYER
LU80284A LU80284A1 (en) 1977-12-27 1978-09-25 PROCESS FOR MANUFACTURING AN EMBOSSED THERMOPLASTIC AREA COVERING
DK424478A DK424478A (en) 1977-12-27 1978-09-25 PROCEDURE FOR PREPARING AN IMPROVED THERMOPLASTIC SURFACE
CA312,443A CA1101795A (en) 1977-12-27 1978-10-02 Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating
BE78190881A BE870980A (en) 1977-12-27 1978-10-03 PROCESS FOR OBTAINING A POLYMERIZED COATING ON A STAMPED VINYL SURFACE
FR7830157A FR2413135A1 (en) 1977-12-27 1978-10-24 PROCESS FOR OBTAINING A POLYMERIZED COATING ON A STAMPED VINYL SURFACE
NO783906A NO152362C (en) 1977-12-27 1978-11-20 PROCEDURE FOR PREPARING A FLOOR COVER WITH AN EMBROIDERED SURFACE
JP15430678A JPS5494565A (en) 1977-12-27 1978-12-15 Method of making embossed vinyl cover with clear photopolymerization coating
GB7849720A GB2010700B (en) 1977-12-27 1978-12-21 Process for the manufacture of embossed surface covering and surface covering produced thereby
NL7812536.A NL166994C (en) 1977-12-27 1978-12-22 PROCESS FOR THE MANUFACTURE OF A RELIEF-INSERTED THERMOPLASTIC SURFACE COATING WITH A BRIGHT, DURABLE, TOUGH, STAIN RESISTANT LAYER FROM PHOTOPOLYMERISABLE MATERIAL.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/864,464 US4150169A (en) 1977-12-27 1977-12-27 Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating

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US4150169A true US4150169A (en) 1979-04-17

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US05/864,464 Expired - Lifetime US4150169A (en) 1977-12-27 1977-12-27 Method for manufacturing an embossed vinyl surface covering having a clear photopolymerized coating

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US (1) US4150169A (en)
JP (1) JPS5494565A (en)
AU (1) AU504396B1 (en)
BE (1) BE870980A (en)
CA (1) CA1101795A (en)
DE (1) DE2840581C3 (en)
DK (1) DK424478A (en)
FR (1) FR2413135A1 (en)
GB (1) GB2010700B (en)
LU (1) LU80284A1 (en)
NL (1) NL166994C (en)
NO (1) NO152362C (en)
SE (1) SE431831C (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4206249A (en) * 1977-09-06 1980-06-03 Nihon Dixie Company Limited Process for producing a paper container having high impermeability to liquid
US4230793A (en) * 1977-11-21 1980-10-28 Ciba-Geigy Corporation Process for the production of solder masks for printed circuits
US4329421A (en) * 1980-01-07 1982-05-11 Armstrong Cork Company Use of flashed radiant energy in producing relief images in resinous coating
US4425403A (en) 1981-03-26 1984-01-10 Toray Industries, Inc. Coated plastic article
WO1993005227A3 (en) * 1991-09-12 1993-04-15 Mannington Mills Resilient floor covering and method of making same
US20030148126A1 (en) * 2002-02-01 2003-08-07 Dong Tian Multi-functional unsaturated polyester polyols
US20050176321A1 (en) * 2003-10-14 2005-08-11 Crette Stephanie A. Fiber wear layer for flooring and other products
US11667080B2 (en) 2019-04-29 2023-06-06 Mighty Buildings, Inc. System for obtaining a photopolymerized prepolymer
US11891465B2 (en) 2019-04-29 2024-02-06 Mighty Buildings, Inc. System for obtaining a photopolymerized prepolymer

Families Citing this family (2)

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Publication number Priority date Publication date Assignee Title
DE3433382A1 (en) * 1984-09-12 1986-03-20 Pegulan-Werke Ag, 6710 Frankenthal METHOD AND DEVICE FOR CONTINUOUSLY COATING PLASTIC FLOORING WITH STRUCTURED SURFACE
DE3504307A1 (en) * 1985-02-08 1986-08-14 Pegulan-Werke Ag, 6710 Frankenthal METHOD FOR PRODUCING AN EMBOWDED, DRAWABLE, FOAM COMPOSITE FILM

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US3518141A (en) * 1967-10-30 1970-06-30 Eastman Kodak Co Method of applying photographic coatings to a moving web with a spliced joint
JPS5012084A (en) * 1973-04-11 1975-02-07
US3924023A (en) * 1973-04-03 1975-12-02 Gaf Corp Floor tile production and products
US4016334A (en) * 1975-02-18 1977-04-05 Celanese Corporation Method of applying high adhesion ultraviolet curable coatings and coated articles

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Publication number Priority date Publication date Assignee Title
US3518141A (en) * 1967-10-30 1970-06-30 Eastman Kodak Co Method of applying photographic coatings to a moving web with a spliced joint
US3924023A (en) * 1973-04-03 1975-12-02 Gaf Corp Floor tile production and products
JPS5012084A (en) * 1973-04-11 1975-02-07
US4016334A (en) * 1975-02-18 1977-04-05 Celanese Corporation Method of applying high adhesion ultraviolet curable coatings and coated articles

Non-Patent Citations (1)

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Title
Toensmeier; Patrick A., "Curtain Coating for Corrugated Blanks," Packaging, Oct. 1960, p. B-13.

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4206249A (en) * 1977-09-06 1980-06-03 Nihon Dixie Company Limited Process for producing a paper container having high impermeability to liquid
US4230793A (en) * 1977-11-21 1980-10-28 Ciba-Geigy Corporation Process for the production of solder masks for printed circuits
US4329421A (en) * 1980-01-07 1982-05-11 Armstrong Cork Company Use of flashed radiant energy in producing relief images in resinous coating
US4425403A (en) 1981-03-26 1984-01-10 Toray Industries, Inc. Coated plastic article
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Also Published As

Publication number Publication date
JPS5437019B2 (en) 1979-11-13
NL7812536A (en) 1979-06-29
BE870980A (en) 1979-02-01
NO152362B (en) 1985-06-10
GB2010700B (en) 1982-06-16
GB2010700A (en) 1979-07-04
NO152362C (en) 1985-09-18
NO783906L (en) 1979-06-28
DK424478A (en) 1979-06-28
NL166994C (en) 1981-10-15
FR2413135A1 (en) 1979-07-27
SE7809967L (en) 1979-06-28
NL166994B (en) 1981-05-15
JPS5494565A (en) 1979-07-26
SE431831B (en) 1984-03-05
DE2840581B2 (en) 1980-01-03
SE431831C (en) 1985-12-23
LU80284A1 (en) 1979-03-16
FR2413135B1 (en) 1980-09-05
CA1101795A (en) 1981-05-26
DE2840581A1 (en) 1979-06-28
AU504396B1 (en) 1979-10-11
DE2840581C3 (en) 1980-09-04

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